ATE8893T1 - DIHYDRO-AS-TRIAZINO(5,6-C)QUINOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICALS CONTAINING THESE COMPOUNDS. - Google Patents
DIHYDRO-AS-TRIAZINO(5,6-C)QUINOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICALS CONTAINING THESE COMPOUNDS.Info
- Publication number
- ATE8893T1 ATE8893T1 AT81102906T AT81102906T ATE8893T1 AT E8893 T1 ATE8893 T1 AT E8893T1 AT 81102906 T AT81102906 T AT 81102906T AT 81102906 T AT81102906 T AT 81102906T AT E8893 T1 ATE8893 T1 AT E8893T1
- Authority
- AT
- Austria
- Prior art keywords
- triazino
- dihydro
- general formula
- addition salts
- quinoline derivatives
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 150000003839 salts Chemical class 0.000 abstract 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 230000021736 acetylation Effects 0.000 abstract 3
- 238000006640 acetylation reaction Methods 0.000 abstract 3
- 239000000126 substance Substances 0.000 abstract 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- 239000012345 acetylating agent Substances 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Anesthesiology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1. Claims for the Contracting states : BE, CH/LI, DE, FR, GB, IT, NL, SE Dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula see diagramm : EP0038528,P16,F1 wherein R represents an alkyl radical having 4, 5 or 8 carbon atoms or a phenyl radical and X1 means a hydrogen atom or an acetyl radical and either X2 or X3 represents hydrogen or an acetyl radical and the other of X2 and X3 has no meaning and the dotted lines mean 1 chemical bond each only either the one or the other being present with the further definition that in case X1 represents hydrogen none of X2 and X3 means hydrogen as well as their acid addition salts. 1. Claims for the Contracting state : AT A process for preparing dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula see diagramm : EP0038528,P17,F2 wherein R represents an alkyl radical having 4, 5 or 8 carbon atoms or a phenyl radical and X1 means a hydrogen atom or an acetyl radical and either X2 or X3 represents hydrogen or an acetyl radical and the other of X2 and X3 has no meaning and the dotted lines mean 1 chemical bond each only either the one or the other being present with the further definition that in case X1 represents hydrogen none of X2 and X3 means hydrogen as well as their acid addition salts, characterized in that in a manner known per se one acetylizes acid addition salts of dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula see diagramm : EP0038528,P18,F1 wherein R is as above defined and Z1 represents hydrogen and either Z2 or Z3 means hydrogen and the other of Z2 and Z3 has no meaning and the dotted lines mean 1 chemical bond each only either the one or the other being present with acetic acid and/or derivatives of it active regarding acetylation as acetylating agents and optionally one converts possibly obtained monoacetyl-dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula I or acid addition salts thereof, respectively, optionally after liberating the former from the latter or converting the latter into the former, respectively, by further acetylation with acetic acid and/or derivatives of it active regarding acetylation as acetylating agents into diacetyldihydro-as-triazino[5,6-c]quinoline derivatives having the general formula I or acid addition salts thereof, respectively, whereafter in a manner known per se optionally one converts the obtained dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula I with inorganic or organic acids into acid addition salts or optionally one converts the obtained acid addition salts of the dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula I with bases into the free dihydro-as-triazino[5,6-c]quinoline derivatives having the general formula I or in other acid addition salts, respectively.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU80939A HU181689B (en) | 1980-04-18 | 1980-04-18 | Process for producing new dihydro-as-triazino-square bracket-5,6-c-square bracket closed-quinoline derivatives |
| EP81102906A EP0038528B1 (en) | 1980-04-18 | 1981-04-15 | Dihydro-as-triazino(5,6-c)quinoline derivatives, process for their preparation and pharmaceutical compositions containing these compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE8893T1 true ATE8893T1 (en) | 1984-08-15 |
Family
ID=10952123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT81102906T ATE8893T1 (en) | 1980-04-18 | 1981-04-15 | DIHYDRO-AS-TRIAZINO(5,6-C)QUINOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICALS CONTAINING THESE COMPOUNDS. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4342766A (en) |
| EP (1) | EP0038528B1 (en) |
| JP (1) | JPS56166190A (en) |
| AT (1) | ATE8893T1 (en) |
| AU (1) | AU540758B2 (en) |
| CS (1) | CS221293B2 (en) |
| DD (1) | DD158399A5 (en) |
| DE (1) | DE3165346D1 (en) |
| DK (1) | DK170581A (en) |
| ES (1) | ES8203369A1 (en) |
| FI (1) | FI70896C (en) |
| GR (1) | GR74516B (en) |
| HU (1) | HU181689B (en) |
| SU (1) | SU1014475A3 (en) |
| YU (1) | YU100981A (en) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3721670A (en) * | 1971-04-05 | 1973-03-20 | Morton Norwich Products Inc | 3-substituted-as-triazino(5,6-c)quinolines |
| HU165678B (en) * | 1972-05-05 | 1974-10-28 | ||
| HU165520B (en) * | 1972-05-05 | 1974-09-28 | ||
| HU165677B (en) * | 1972-05-05 | 1974-10-28 |
-
1980
- 1980-04-18 HU HU80939A patent/HU181689B/en not_active IP Right Cessation
-
1981
- 1981-04-14 DK DK170581A patent/DK170581A/en active IP Right Grant
- 1981-04-15 AT AT81102906T patent/ATE8893T1/en active
- 1981-04-15 DE DE8181102906T patent/DE3165346D1/en not_active Expired
- 1981-04-15 ES ES502078A patent/ES8203369A1/en not_active Expired
- 1981-04-15 EP EP81102906A patent/EP0038528B1/en not_active Expired
- 1981-04-16 FI FI811193A patent/FI70896C/en not_active IP Right Cessation
- 1981-04-16 US US06/254,763 patent/US4342766A/en not_active Expired - Lifetime
- 1981-04-16 AU AU69645/81A patent/AU540758B2/en not_active Ceased
- 1981-04-16 DD DD81229303A patent/DD158399A5/en unknown
- 1981-04-16 YU YU01009/81A patent/YU100981A/en unknown
- 1981-04-17 JP JP5727081A patent/JPS56166190A/en active Pending
- 1981-04-17 CS CS812952A patent/CS221293B2/en unknown
- 1981-04-17 SU SU813273760A patent/SU1014475A3/en active
- 1981-04-17 GR GR64727A patent/GR74516B/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU540758B2 (en) | 1984-12-06 |
| ES502078A0 (en) | 1982-04-01 |
| DE3165346D1 (en) | 1984-09-13 |
| HU181689B (en) | 1983-11-28 |
| DD158399A5 (en) | 1983-01-12 |
| US4342766A (en) | 1982-08-03 |
| EP0038528B1 (en) | 1984-08-08 |
| FI70896B (en) | 1986-07-18 |
| FI811193L (en) | 1981-10-19 |
| DK170581A (en) | 1981-10-19 |
| YU100981A (en) | 1983-10-31 |
| JPS56166190A (en) | 1981-12-21 |
| FI70896C (en) | 1986-10-27 |
| CS221293B2 (en) | 1983-04-29 |
| GR74516B (en) | 1984-06-29 |
| AU6964581A (en) | 1981-10-22 |
| ES8203369A1 (en) | 1982-04-01 |
| SU1014475A3 (en) | 1983-04-23 |
| EP0038528A1 (en) | 1981-10-28 |
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